WO1992002244A1 - Accumulation d'acides amines et de peptides dans des liposomes - Google Patents

Accumulation d'acides amines et de peptides dans des liposomes Download PDF

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Publication number
WO1992002244A1
WO1992002244A1 PCT/US1991/005281 US9105281W WO9202244A1 WO 1992002244 A1 WO1992002244 A1 WO 1992002244A1 US 9105281 W US9105281 W US 9105281W WO 9202244 A1 WO9202244 A1 WO 9202244A1
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WIPO (PCT)
Prior art keywords
liposomes
peptide
gradient
amino acid
lysine
Prior art date
Application number
PCT/US1991/005281
Other languages
English (en)
Inventor
Ajoy Chakrabarti
Ian Clark-Lewis
Pieter R. Cullis
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The Liposome Company, Inc.
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Filing date
Publication date
Application filed by The Liposome Company, Inc. filed Critical The Liposome Company, Inc.
Priority to EP91915597A priority Critical patent/EP0555229B1/fr
Priority to AU84365/91A priority patent/AU660288B2/en
Priority to DE69120089T priority patent/DE69120089T2/de
Publication of WO1992002244A1 publication Critical patent/WO1992002244A1/fr
Priority to GR960402044T priority patent/GR3020686T3/el
Priority to HK98106742A priority patent/HK1007497A1/xx

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/10—Dispersions; Emulsions
    • A61K9/127—Liposomes
    • A61K9/1277—Processes for preparing; Proliposomes
    • A61K9/1278—Post-loading, e.g. by ion or pH gradient
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/10—Peptides having 12 to 20 amino acids
    • A61K38/105—Bombesin; Related peptides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/22—Hormones
    • A61K38/2207—Gastrins; Cholecystokinins [CCK]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/22—Hormones
    • A61K38/25—Growth hormone-releasing factor [GH-RF], i.e. somatoliberin
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S436/00—Chemistry: analytical and immunological testing
    • Y10S436/829—Liposomes, e.g. encapsulation
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
    • Y10T428/2984—Microcapsule with fluid core [includes liposome]

Definitions

  • the liposomes can be prepared in the absence of the drug, problems with drug release during storage, or dia-g degradation during liposomal preparation can be avoided.
  • Intraliposomal drug accumulation in response to pH gradients is believed to occur in a manner similar to that of other weak bases, 0 for example, the pH gradient probe methylamine. Methylamine equilibrates across liposomal membranes in the uncharged form, and reionizes according to the Henderson- Hasselbach relationship of the pH of its environment. The equilibrium distribution reflects the transmembrane pH gradient, and its redistribution can be used to 5 measure these gradients.
  • Liposomes are completely closed lipid bilayer membranes which contain entrapped aqueous volume. Liposomes are vesicles which may be unilamellar (single membrane) or multilamellar (onion-like structures characterized by multiple membrane bilayers, each separated from the next by an aqueous layer) .
  • the bilayer is composed of two lipid monolayers having a hydrophobic "tail” region and a hydrophilic "head” region. In the membrane bilayer, the hydrophobic (nonpolar) "tails" of the lipid monolayers orient toward the center of the bilayer, whereas the hydrophilic (polar) "heads” orient toward the aqueous phase.
  • amino acids and peptides which exhibit weak acid or base characteristics.
  • the amino acids and peptides of this aspect of the invention are more specifically those wherein the C terminal and other carboxyl functions have been modified by substitution thereof, and associated with a functional group such as for example an ester or an amide. More specifically, basic amino acids and peptides of the invention have been modified to methyl ester, ethyl ester or amide forms.
  • transmembrane concentration gradient occurs for certain amino acids and peptides wherein the C-terminal carboxyl function is substituted, wherein the amino acid or peptide would exhibit weak acid or base characteristics, and more specifically, wherein such amino acid or peptide carboxyl function is modified to a non-acidic group such as an amide or a methyl ester.
  • Such amino acid and peptide derivatives exhibit weak base characteristics.
  • Such amino acids and peptides load into LUVs by methods of the invention in response to a transmembrane concentration gradient (for example a transmembrane pH gradient) (inside acidic).
  • the methods of the invention result in transmembrane concentration gradient-driven loading for the amino acid derivatives lysine methyl ester, lysine amide, lysine ethyl ester, and the peptides Bombesin
  • FIGURE 1 graphically represents the time course of lysine methyl ester into 100 nm EPC vesicles bearing a 7.5/4.0
  • FIGURE 2 graphically represents the time course of uptake of lysine methyl ester into 100 nm EPC:cholesterol vesicles (55:45 mole%) bearing a 7.5/4.0 (external/internal) pH gradient. Uptake was conducted at 4°C (open circles), 20°C (open triangles), and 37°C (open squares). The external concentration of lysine methyl ester was 2.0 mM.
  • FIGURE 3 graphically represents the time course of uptake of Lys-Tyr-Trp-Trp-Phe-Amide into 100 nm EPC vesicles bearing a 7.5/4.0 (external/internal) (open squares) and a 7.5/7.5 (external/internal) (open circles) pH gradient. Uptake was conducted at 23°C. The external concentration of Lys-Tyr-Trp-Trp -Phe-Amide was 76 uM.
  • the present invention relates to liposomal compositions having a pH gradient, such liposomes exhibiting markedly increased accumulation of amino acids and peptides as expected from the Henderson-Hasselbach relationship, by formulating the liposomes utilizing a first internal aqueous buffer and a second external aqueous buffer, the first and second buffers differing as to ionic (proton) concentration.
  • the present invention is further directed to a method for loading liposomes with a C-terminal carboxyl function substituted amino acid or peptide, therefore wherein the amino acid or peptide would exhibit weak acid or base characteristics, and more specifically, wherein such amino acid or peptide carboxyl function is modified to a non-acidic group such as an amide or a methyl ester.
  • Such amino acid and peptide derivatives exhibit weak base characteristics.
  • the loading includes preparing liposomes having a concentration gradient of one or more charged species across their membranes, said concentration gradient being capable of generating a transmembrane potential having an orientation which will cause the peptide to be loaded into the liposomes, and admixing the amino acid or peptide with the liposomes.
  • the liposomes are those that can be formed by any method but are preferably large unilamellar vesicles.
  • the concentration gradient is formed by encapsulating a first medium in the liposomes, said medium having a first concentration of the one or more charged species, and suspending the liposomes in a second medium having a second concentration of the one or more charged species .
  • a concentration gradient can be for example, a pH gradient.
  • amino acid and peptide derivatives which can be loaded by the transmembrane concentration gradient method of the invention include the amino acid derivatives lysine methyl ester, lysine amide, lysine ethyl ester, and the peptides Bombesin
  • Gastrin-Related Peptide N-t-BOC-Trp-Met-Asp-Phe-Amide
  • Growth Hormone Releasing Peptides Tyr-Gly-Trp-Phe-Phe-.Amide and Trp-Ala-Trp-Phe-Ala -Amide,and Growth Hormone Releasing Factor
  • compositions comprising such
  • the transmembrane potential can be produced by creating a concentration gradient of one or more charged species across the liposomes membranes, such as for example H ions, wherein the concentration gradient is a pH gradient.
  • the liposome compositions of the present invention may comprise phospholipids such as egg phosphatidylcholine (EPC), hydrogenated soy phosphatidylcholine, distearoylphosphatidylcholine, dimyristoylphosphatidylcholine, or diarachidonylphosphatidylcholine ⁇ y- among others, and may additionally comprise a number of steroidal compositions, as well as other compositions.
  • EPC egg phosphatidylcholine
  • hydrogenated soy phosphatidylcholine distearoylphosphatidylcholine
  • dimyristoylphosphatidylcholine dimyristoylphosphatidylcholine
  • diarachidonylphosphatidylcholine ⁇ y- among others may additionally comprise a number of steroidal compositions, as well as other compositions.
  • the liposomal compositions additionally comprise steroidal compositions
  • these may include cholesterol, which may be used preferably in a 55:45 (lipid:steroidal lipid) w/w ratio.
  • the present invention discloses efficient trapping of amino acids and peptides in liposomes exhibiting a transmembrane ionic gradient, preferably a transmembrane pH gradient.
  • amino acid and peptide derivatives which can be loaded by the transmembrane concentration gradient method of the invention include the amino acid derivatives lysine methyl ester, lysine amide, lysine ethyl ester, and the peptides Bombesin
  • the liposomes of the present invention may be formed by any of the methods known in the art, but preferably they are formed according to the procedures disclosed in Bally et al., PCT Application No. US86/01102, published February 27, 1986 and Mayer et al. PCT Application No. US88/00646, published September 7, 1988. These techniques allow the loading of liposomes with ionizable agents to achieve interior concentrations considerably greater than otherwise expected from the agents' solubility in aqueous solution at neutral pH and/or concentrations greater than can be obtained by passive entrapment techniques.
  • a transmembrane ion (pH) gradient is created between the internal and external membranes of the liposomes and the agent is loaded into the liposomes by means of the ion (pH) gradient, which drives the uptake.
  • the transmembrane gradient is generated by creating a concentration gradient for one or more charged species, for example Na+, C1-, K+, Li+, OH- and preferably H+, across the liposome membranes, such that the ion gradient drives the uptake of ionizable agents across the membranes.
  • transmembrane ion (H+) gradients are preferably employed to produce the ion gradient and load the agents, which tend to have weakly basic nitrogen groups, into the liposomes.
  • liposomes are preferably first formed in an aqueous buffer solution.
  • the first solution is either acidic or basic, depending upon whether the agent to be loaded produces a charged species at basic or acidic pH.
  • a charged species is produced at low pH, i.e., a pH of 2.0 to 5.0, preferably a pH of 4.0.
  • the buffer solution external to the liposomes is then modified to a pH significantly above the pH of the internal buffer solution, preferably at least 3.0 to 4.0 pH units above the internal buffer solution.
  • the modification of the external buffer results in a pH gradient which drives the accumulation of the agent within the liposome.
  • the agent will pass through the lipid layer(s) of the liposome in its uncharged form much more readily than it will in its charged (protonated, in the case of weakly basic agents) form.
  • uncharged agent in the external buffer will readily pass through the liposome into the internal buffer, become protonated, and remain within the liposome as a "trapped" protonated molecule which does not readily pass through the liposome layer(s). Agent will thus concentrate in the liposome as a function of the pH gradient between the internal and external buffer solutions.
  • the first aqueous buffer solution will surround the liposomes as they are formed, resulting in the buffer solution being internal and external to the liposomes.
  • the original external buffer solution may be acidified or alkalinized so that the concentration of charged species differs from the internal buffer, or alternatively, the external buffer may be replaced by a new external medium having different charge species.
  • the replacement of the external medium can be accomplished by various techniques, such as by passing the liposome preparation through a gel filtration column, e.g., a Sephadex column, which has been equilibrated with the new medium, or by dialysis or related techniques.
  • liposome compositions are preferred which are formed utilizing a first internal buffer solution of acidic character (pH 3.0 to 5.0) and a second external buffer solution, the pH of which is preferably between 6.5 and 8.0, preferably 7.5.
  • the low pH of the internal buffer relative to a more basic or neutral pH of the external buffer produces a transmembrane gradient which acts to drive the accumulation of the agent in the liposome.
  • Lipids which can be used in the liposome formulations of the present invention include synthetic or natural phospholipids and may include phosphatidylcholine (PC), phosphatidylethanolamine (PE), phosphatidyiserine (PS), phosphatidylglycerol (PG), phosphatidic acid (PA), phosphatidylinositol (PI), sphingomyelin (SPM) and cardiolipin, among others, either alone or in combination.
  • the phospholipids useful in the present invention may also include dimyristoylphosphatidylcholine (DMPC) and dimyristoylphosphatidylglycerol (DMPG) .
  • distearylphosphatidylcholine DSPC
  • dipalmitoylphosphatidylcholine DPPC
  • hydrogenated soy phosphatidylcholine HSPC
  • Dimyristoylphosphatidylcholine DMPC
  • diarachidonoyl- phosphatidylcholine DAPC
  • T transition temperatures
  • such lipids are preferably heated to about their T or temperatures slightly higher, e.g., up to 5°C higher than the T in order to make these liposomes.
  • a steroidal component may be a-, ed to the liposome, regardless of the phospholipid chosen.
  • a steroidal component may for example be selected from the group consisting of cholesterol, cholestanol, coprostanol or cholestane.
  • PEG-cholesterols polyethylene glycol derivatives of cholesterol
  • CHS cholesterol hemisuccin.te
  • CHS- and THS-containing liposomes and their tris salt forms may generally be prepared by any method known in the art for preparing liposomes containing sterols. Any of the above-mentioned sterols may be used in liposomes, so long as the resultant phospholipid-sterol mixture yields stable liposomes. In particular, see the procedures of Janoff, et al., U.S. Patent No. 4,721,612, issued January 26, 1988, entitled “Steroidal Liposomes", and Janoff, et al., PCT Publication No.
  • cholesterol in an amount equal to 30 mole% to 45 mole% by weight of the lipid comprising the liposome is preferably used in combination with any of the above-named phospholipids or phospholipid/steroid combinations.
  • Such compositions should, in general, prevent the undesired rapid release of accumulated agent from the liposome.
  • Any combination of membrane-stabilizing component and lipid may be used which prevents rapid release of agents from the liposome, and one of ordinary skill in the art will be able to modify the membrane-stabilizing component and the phospholipid to formulate liposomes which prevent rapid release of the agent.
  • liposomes comprising either phosphatidylcholine or a mixture of 45 mole % by weight cholesterol and 55 mole % by weight phosphatidylcholine are used in this aspect of the present invention.
  • MLVs multilamellar vesicles
  • SPLVs stable plurilamellar vesicles
  • REVs reverse phase evaporation vesicles
  • MLVs are extruded through filters forming large unilamellar vesicles (LUVs) of sizes dependent upon the filter size utilized.
  • LUVs large unilamellar vesicles
  • polycarbonate filters of 30, 50, 60, 100, 200 or 800 nm pores may be used.
  • the liposome suspension may be repeatedly passed through the extrusion device resulting in a population of liposomes of homogeneous size distribution.
  • the filtering may be performed through a straight-through membrane filter (a Nucleopore polycarbonate filter) or a tortuous path filter (e.g. a Nucleopore filter membrafil filter (mixed cellulose esters) of 0.1 urn size), or by alternative size reduction techniques such as homogenization.
  • the size of the liposomes may vary from 0.03 to above about 2 microns in diameter; preferably 0.05 to 0.3 microns and most preferably 0.1 to 0.2 microns.
  • the size range includes liposomes that are MLVs, SPLVs, or LUVs.
  • the preferred liposomes are those which are unilamellar liposomes of 0.1 to 0.2 microns.
  • a number of lipids may be used to form liposomes having a gel to liquid crystalline Tc above ambient temperature.
  • an extruder having a heating barrel or thermojacket may be employed.
  • Such a device serves to increase the liposome suspension temperature allowing extrusion of the LUVs.
  • the lipids which are used with the thermojacketed extruder are, for example, DSPC, DPPC, DMPC and DAPC or mixtures thereof, which may include cholesterol in certain embodiments for preventing the rapid release of agents from the liposome.
  • Liposomes containing DSPC are generally extruded at 65°C, DPPC at 45°C and DAPC at 85°C (5°C above the lipid T ).
  • the preferred liposome for use in the present invention are LUVs of about 0.06 to 0.3 microns in size.
  • a homogeneous population of vesicles is one comprising substantially the same size liposomes, and may have a Gaussian distribution of particle sizes. Such a population is said to be of uniform size distribution, and may be unimodal with respect to size.
  • the term "unimodal" refers to a population having a narrow polydispersity of particle sizes, and the particles are of a single
  • a liposomal population is unimodal if, when measured by quasi elastic light scattering methods, the population approximates to a Gaussian distribution, and if a second order polynomial will fit the natural logarithm of the autocorrelation function of a sample (Koppel, 1972, J. Chem. Phys., 57:4814). The closer this fit, the better the measure of unimodality. The closeness of this
  • Liposomes may be prepared which encapsulate the first aqueous buffer solution having the characteristics described hereinabove.
  • organic solvents may also be used to suspend the lipids.
  • Suitable organic solvents for use in the present invention include those with a variety of polarities and dielectric properties, which solubilize the lipids, for example, chloroform, methanol, ethanol, dimethylsulfoxide (DMSO), methylene choloride, and solvent mixtures such as benzene:methanol (70:30), among others.
  • DMSO dimethylsulfoxide
  • solvent mixtures such as benzene:methanol (70:30)
  • Solvents are generally chosen on the basis of their biocompatability, low toxicity, and solubilization abilities.
  • One preferred embodiment of the present invention is a 3 component liposomal-agent treatment system which allows for highly efficient entrapment of the agent at the clinical site.
  • the agent is one that loads in response to a transmembrane pH gradient where the interior of the liposome is acid
  • the first component of the system comprises liposomes in an acidic aqueous or buffer solution, for example, citric acid buffer (at 300 mM, pH 3.8 to 4.2, preferably 4.0).
  • the second component of the system comprises a relatively basic buffer or aqueous solution, for example, a sodium carbonate or sodium bisphosphate solution, or a sodium chloride/HEPES b ⁇ ered saline solution ("HBS") at ?H 10 to 12, preferably pH 11.5, which serves to become part of the external aqueous or buffer solution of the liposome formulation.
  • a relatively basic buffer or aqueous solution for example, a sodium carbonate or sodium bisphosphate solution, or a sodium chloride/HEPES b ⁇ ered saline solution ("HBS”) at ?H 10 to 12, preferably pH 11.5, which serves to become part of the external aqueous or buffer solution of the liposome formulation.
  • HBS sodium chloride/HEPES b ⁇ ered saline solution
  • the third component (Vial 3) is the agent to be entrapped.
  • the above-described treatment system may be provided as a 3-vial system, the first vial containing the liposomes in acidic medium, the second vial containing the solution of relative alkalinity, and the t.ird vial containing the amino acid or peptide derivative (the agent), as described hereinabove.
  • a similar treatment system may be provided for an agent that loads in response to a transmembrane gradient wherein the internal buffer of the liposomes is relatively basic i.e., has a pH 8.5-11.5.
  • the first vial would contain the liposomes in rel;actively alkaline medium
  • the second vial would contain the solution of relative acidity
  • the third vial the agent to be entrapped.
  • the liposomes may be heated prior to admixing with the amino acid or peptide.
  • the agent may be advantageous to heat the liposomes to facilitate loading, up to some temperature appropriate to the liposome composition and the presence of the amino acid or peptide. Loading, for example, may take place at temperatures of from 4°C to 60°C.
  • the agent is entrapped in or associated with the liposome and then administered to the patient to be treated.
  • the agents are drugs, see Rahman et al., U.S. Patent No. 3,993,754; Sears, U.S. Patent No. 4,145,410; Papahadjopoulos et al., U.S. Patent No. 4,235,871; Schneider, U.S. Patent No. 4,114,179; Lenk et al., U.S. Patent No. 4,522,803; and Fountain et al., U.S. Patent No. 4,588,578.
  • the terms amino acid and peptide, and the term agent are used interchangably.
  • the choice of buffer to use as the internal buffer solution may vary depending upon the agent chosen for loading.
  • One of ordinary skill in the art will be able to assess the relative solubilities of ionized species of a particular agent and the buffer strength to determine the buffer solution to be used as the internal buffer solution.
  • Any buffer solution having the characteristics generally described hereinabove may be used in the present invention, provided that the solution is pharmaceutically compatible, when necessary, i.e., wherein the solution may be administered to the patient without deleterious affects.
  • Typical internal buffer solutions include citric acid, oxalic acid, succinic acid and other organic acid salts being preferred, among others. Citric acid in a concentration ranging from 100 mM to 300 mM is preferred. Most preferably, the citric acid buffer solution has a concentration of 300mM, Typical external buffer solutions may include NaCl, KC1, potassium phosphate, sodium bicarbonate, sodium carbonate, sodium bisphosphate, potassium sulfate, (N-2-Hydroxyethyl Piperazine-N'-2-Ethane Sulfonic Acid) or "HEPES", 2-[N-morpholino] ethane-sulfonic acid or "MES",
  • the preferred external buffer solution is NaCl/HEPES, and more preferably 150 mM Na.SO , 20 mM HEPES at pH 7.5.
  • Loading efficiencies of agents utilizing the present invention generally range from 20% up to 100%, preferably at least 50%.
  • the loading efficiencies for agents according to the present invention are as expected from the Henderson-Hasselbach relationship.
  • certain agents see Comparative Examples 13, 14 and 15 appear, in certain cases, not to accumulate at all.
  • the liposomes formed by the procedures of the present invention may be lyophilized or dehydrated at various stages of formation.
  • the lipid film may be lyophilized after removing the solvent and prior to adding the agent or forming the liposomes through hydration of the film.
  • Such dehydration may be carried out by exposure of the lipid or liposome to reduced pressure thereby removing all suspending solvent.
  • the liposomes themselves may be dehydrated by any of a number of methods. They may be dehydrated in the presence of a hydrophilic agent according to the procedures of Bally et al, PCT Publication No. 86/01102, published February 27, 1986, entitled “Encapsulation of Antineoplastic Agents in Liposomes", Janoff et al., PCT Publication No. 86/01103, published February 27, 1986, entitled “Dehydrated Liposomes", Schneider et al., in U.S. Patent No. 4,229,360, issued October 29, 1980 and Mayer, et al. PCT Publication No. 88/06442, published September 7, 1988, relevant portions of which are incorporated by reference herein.
  • the hydrated liposome preparation may also be dehydrated by placing it in surrounding medium in liquid nitrogen and freezing it prior to the dehydration step.
  • Dehydration with prior freezing may be performed in the presence of one or more protective agents, such as sugars in the preparation according to the techniques of Bally, et al., PCT Application No. 86/01103 published February 27, 1986, relevant portions of which are also incorporated by reference herein.
  • the agent may be mixed with a sugar solution in a sugar: lipid weight/weight ratio ranging from 0.5:1 to 100:1, preferably 20:1, without affecting the ability of the liposome to retain loaded agent during rehydration.
  • Other suitable methods may be used in the dehydration of the above-disclosed liposome preparations.
  • the liposomes may also be dehydrated without prior freezing.
  • the liposomes Once the liposomes have been dehydrated, they can be stored for extended periods of time until they are to be used.
  • the appropriate temperature for storage will depend on the lipid formulation of the liposomes and the temperature sensitivity of encapsulated materials.
  • amino acids and peptides are heat labile, and thus dehydrated liposomes containing such agents should preferably be stored under refrigerated conditions e.g. at 4°C, so that the potency of the agent is not lost.
  • the dehydration process is preferably carried out at reduced temperatures, rather than at room temperature.
  • rehydration is accomplished by simply adding an aqueous solution, e.g., distilled water or an appropriate buffer, to the liposomes and allowing them to rehydrate.
  • the liposomes can be resuspended into the aqueous solution by gentle swirling of the solution.
  • the rehydration can be performed at room temperature or at othf temperatures appropriate to the composition of the liposomes and tneir internal contents.
  • the concentration gradient used to generate the transmembrane pH gradient can be created either before dehydration or after rehydration using the external medium exchange techniques described above.
  • tiie liposomes may be dehydrated prior to establishing the transmembrane pH gradient, for example, dehydrated from their first external medium.
  • the pH gradient can be established by admixing the liposomes with the second external medium of relatively acidic or basic pH.
  • the agent can be admixed with the liposomes simultar-ously with or following the establishment of the pH gradient.
  • the liposomes may be rehydrated by admixing them with an aqueous solution of neutral pH.
  • the rehydration step would proceed by adding the NaCl/HEPES buffer, and the agent, for example, lysine methyl ester.
  • liposomes containing the amino acid and peptide formulations of the present invention may be used therapeutically in mammals, especially humans, in the treatment of a number of disease states or pharmacological conditions which require sustained release formulations as well as repeated administration.
  • the mode of administration of the liposomes containing the agents of the present invention may determine the sites and cells in the organism to which the compound may be delivered.
  • the liposomes of the present invention may be administered alone but will generally be administered in admixture with a pharmaceutical carrier selected with regard to the intended route of administration and standard pharmaceutical practice.
  • the preparations may be injected parenterally, for example, intravenously.
  • parenteral administration they can be used, for example, in the form of a sterile aqueous solution which may contain other solutes, for example, enough salts or glucose to make the solution isotonic, should isotonicity be necessary or desired.
  • the liposomes of the present invention may also be employed subcutaneously or intramuscularly. Other uses, depending upon the particular properties of the preparation, may be envisioned by those skilled in the art.
  • the liposomal formulations of the present invention can be used in the form of tablets, capsules, losenges, troches, powders, syrups, elixirs, aqueous solutions and suspensions, and the like.
  • carriers which can be used include lactose, sodium citrate and salts of phosphoric acid.
  • Various disintegrants s" ⁇ ' ⁇ as starch, lubricating agents, and talc are commonly used in tablets.
  • useful diluents are lactose and high molecular weight polyethylene glycols.
  • the active ingredient is combined with emulsifying and suspending agents.
  • the liposomal formulations of the present invention may be incorporated into dosage forms such as gels, oils, emulsions, and the like. These formulations may be administered by direct application as a cream, paste, ointment, gel, lotion or the like.
  • the prescribing physician will ultimately determine the appropriate dosage of the neoplastic drug for a given human subject, and this can be expected to vary according to the age, weight and response of the individual as well as the pharmacokinetics of the agent used.
  • the nature and severity of the patient's disease state or condition will influence the dosage regimen. While it is expected that, in general, the dosage of the drug in liposomal form will be about that employed for the free drug, in some cases, it may be necessary to administer dosages outside these limits.
  • EPC Egg phosphatidylcholine
  • Lysine methyl ester was purchased from Sigma Chemical Co.
  • the hydrophobic pentapeptide (H_N -Ala-Met-Leu-Trp-Ala-COO; where the carboxyl function was modified to be a methyl ester or amide) was synthesized using the solid phase synthesis method of de Kroon et al., 1989, BBA, 981:371.
  • Multilamellar vesicles were produced by hydrating 50 mg EPC in 1.0 ml citrate (300mM) buffer at pH 4.0. The MLVs were frozen in liquid nitrogen and thawed in water at 50-60°C for five freeze-thaw cycles.
  • the resulting MLVs were extruded ten times through two stacked lOOnm pore size polycarbonate filters (Nuclepore) employing a device obtained from Lipex Biomembranes Inc. (Vancouver, Canada) as set forth in Hope et al., 1985, BBA, 812:55.
  • the resulting large unilamellar vesicles (LUVs) were 108 nm in diameter as determined by quasielastic light scattering (QELS) employing a NIC0MP particle sizer.
  • QELS quasielastic light scattering
  • the LUVs in the pH 4.0 media were passed down a 10 cm Sephadex G-50 (medium) column previously equilibrated with 150 mM NaCl, 20 mM HEPES (pH 7.5) (Hepes buffered saline or "HBS"), to generate the pH 7.5/4.0 exterior/interior pH gradient.
  • HEPES pH 7.5
  • HBS Hepes buffered saline
  • Uptake of the lysine methyl ester was initiated by first dissolving 0.47 mg of the lysine methyl ester in 1.0 ml of HBS medium 2.0 mM lysine methyl ester) to which 0.25 ml of the LUVs exhibiting the pH gradient were added.
  • the liposomes were incubated at 23°C and aliquots of 0.1 ml were removed at selected times (see Figure 1) from this incubation mixture, and untrapped material removed by passage through 1 ml (dry) Sephadex G-50 column, centrifuged for 1 minute at 2500 rpm.
  • Example 1 The methods of Example 1 were repeated wherein the LUVs in the pH 4.0 media were passed down a 10 cm Sephadex G-50 (medium) column previously equilibrated with 300 mM citrate buffer, at pH 4.0, thus generating no pH gradient.
  • Lysine methyl ester concentrations inside the LUVs of Examples 1 and 2 were determined by a modification of the technique employed by Hope and Cullis, 1987, J. Biol. Chem., 262:4360, employing TNBS (trinitrobenzenesulfonic acid) to label primary amino groups of lysine methyl ester.
  • the buffer used for the labelling was lOO M NaHCO , 50 mM H BO , at pH 10.0.
  • a reference cuvette containing 2.5 ml of buffer (pH 10.0) was placed in the reference beam.
  • the sample cuvette contained 2.5 ml of buffer (pH 10.0) with 0.5 mM TNBS aliquots (50 ul) of vesicles containing lysine methyl ester were then added. The resulting change in absorbance was measured at 420 nm after incubation in the dark for 1 hour. Triton X-100 (200 ul, 0.5%) was added to both cuvettes to solubilize the vesicles and thus expose all primary amino groups present to the TNBS. The absorbance in the presence of detergent was taken to represent 100% labelling.
  • Phospholipid concentrations were calculated by a modification of the method of Fiske and Subbarow, 1925, J. Biol. Chem., 66:375. Typical phospholipid concentrations were approximately 3.0 mM. Example 6
  • the amino acid loaded quickly with maximal levels being loaded with the first 5-10 minutes of incubation.
  • a corresponding decrease in the measured pH gradient was also observed, represented by the closed circles and read using the scale on the right axis, wherein the gradient dropped from 3.5 to 1 pH unit; such drop in the residual pH gradient being due to protonation of the methyl ester after traversal of the membrane in the neutral form.
  • the maximal concentrations entrapped were about 85 nmoles lysine me. l ester/umole phospholipid. This high level of uptake was maintained for at least 24 hours with no leakage of the lysine methyl ester.
  • EPC:cholesterol vesicles (55:45 mole%) were made by dissolving 43 mg EPC and 17 mg cholesterol in 1.0 ml of chloroform. The chloroform was then removed under a stream of nitrogen and by subsequent storage under reduced pressure. The methods of Example 1 were employed using 20 ml of citrate buffer (pH 4.0) to produce frozen-and-thawed MLVs which were then likewise extruded to form LUVs. In the case of EPC:cholesterol vesicles, the extrusion step took place at 65°C.
  • Figure 2 is a graphic representation of the time course of the amino acid loading into LUVs exhibiting the pH gradient of 7.5/4.0 (external/internal).
  • the time course of uptake is reported at uptake incubation temperatures of 37°C (open squares), 20°C (open triangles), and 4°C (open circles).
  • Very high levels of loading (approximately 70 nmoles/umole phospholipid) were achieved within 10 minutes at 37°C, 1 hour at 20°C, and potentially after more than 22 hours at 4°C.
  • the amount of lysine methyl ester entrapped was again found to remain quite stable, even after long time periods (more than 20 hours) at elevated temperatures (37°C).
  • Example 1 The methods of Example 1 were employed wherein the amino acid
  • Lysine ethyl ester was loaded into LUVs following incubation at 23°C for 1 hour. Loading of this amino acid derivative occurred at a value of 378.0 nmoles peptide/umole phospholipid.
  • Example 1 The methods of Example 1 were employed wherein the peptide Bombesin (pGlu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val-Gly-His-Leu- Met-NH.) was loaded into LUVs following incubation at 23°C for 1 hour. Loading of this peptide derivative occurred to a value of 34.6 nmoles peptide/umole phospholipid. 0
  • Example 1 The methods of Example 1 were employed wherein Gastrin-Related Peptide (N-t-BOC-Trp-Met-Asp-Phe-NH ) was incubated with the LUVs - at 23°C for 1 hour. Following this incubation time period, 25.1 nmoles peptide/umole phospholipid was loaded into the L'.T'/s.
  • Gastrin-Related Peptide N-t-BOC-Trp-Met-Asp-Phe-NH
  • Example 1 The methods of Example 1 were employed wherein 74 ug of the peptide Growth Hormone Releasing Factor Fragment (Lys-Tyr-Trp-Trp- Phe-NH-) was incubated with the LUVs at 60°C for 2 hours. Following this incubation time period, 195.0 nmoles peptide/umole phospholipid was loaded into the LUVs.
  • Example 1 The methods of Example 1 were employed wherein 74 ug of the peptide Growth Hormone Releasing Factor Fragment (Lys-Tyr-Trp-Trp- Phe-NH ) was incubated with the LUVs at 23°C for 2 hours, the results of which are represented in Figure 3. Following the 2-hour incubation time period, about 55 nmoles peptide/umole phospholipid was loaded into the LUVs.
  • the open squares represent the uptake course with a 7.5/4.0 (external/internal) initial pH gradient, with the closed squares representing the residual pH gradient, as read using the scale on the right axis.
  • the open circles represent the uptake course with no pH gradient, wherein the internal and external solutions were both initially pH 7.5. Comparative Example 13
  • Example 1 The methods of Example 1 were employed wherein 0.48 mg of the amino acid derivative histidine methyl ester (Sigma Chemical Co., St. Louis, M0) was incubated at 23°C with the LUVs. After an incubation of 1 hour, no loading took place (0 nmoles peptide/umole lipid loaded).
  • Example 1 The methods of Example 1 were employed wherein 0.34 mg of the peptide (Lys),.methyl ester was incubated at 23°C with the LUVs.
  • Example 1 The methods of Example 1 were employed wherein 0.95 mg of the peptide (Lys-(Ala).) methyl ester was incubated at 23°C with the LUVs. Following an incubation of about 1 hour, no loading took place (0 nmoles peptide/umoles lipid loaded).

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Abstract

Cette invention concerne des compositions de liposomes ayant un gradient de concentration qui charge dans des liposomes, des acides aminés et des peptides présentant de faibles caractéristiques acides ou basiques. Plus spécifiquement, on peut, à l'aide des procédés de cette invention, charger dans des liposomes, des acides aminés ou des peptides à substitution de la terminaison C. Les liposomes sont, de préférence, de grandes vésicules unilamellaires. On forme le gradient de concentration en encapsulant un premier milieu dans les liposomes, ledit milieu ayant une première concentration d'une ou plusieurs espèces chargées, puis on met en suspension les liposomes dans un deuxième milieu ayant une deuxième concentration d'une ou de plusieurs espèces chargées, comme par exemple un gradient de pH. L'invention concerne également des préparations pharmaceutiques comprenant de tels acides aminés ou peptides à substitution de la terminaison C qui ont été chargés dans les liposomes au moyen du procédé de cette invention.
PCT/US1991/005281 1990-07-31 1991-07-25 Accumulation d'acides amines et de peptides dans des liposomes WO1992002244A1 (fr)

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EP91915597A EP0555229B1 (fr) 1990-07-31 1991-07-25 Accumulation d'acides amines et de peptides dans des liposomes
AU84365/91A AU660288B2 (en) 1990-07-31 1991-07-25 Accumulation of amino acids and peptides into liposomes
DE69120089T DE69120089T2 (de) 1990-07-31 1991-07-25 Anhäufung von aminosäuren und peptiden in liposomen
GR960402044T GR3020686T3 (en) 1990-07-31 1996-07-31 Accumulation of amino acids and peptides into liposomes
HK98106742A HK1007497A1 (en) 1990-07-31 1998-06-25 Accumulations of amino acids and peptides into liposomes

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US5871945A (en) * 1994-11-23 1999-02-16 Icos Corporation Modulators of anchoring protein function
US5629163A (en) * 1994-11-23 1997-05-13 Icos Corporation Calcineurin inhibitory compounds and anchoring protein
US6107104A (en) * 1994-11-23 2000-08-22 Icos Corporation Modulators of anchoring protein function
US5744354A (en) * 1994-11-23 1998-04-28 Icos Corporation Calcineurin inhibitory compounds and anchoring protein to induce IL-2 gene expression
US5807693A (en) * 1994-11-23 1998-09-15 Icos Corporation Calcineurin inhibitory compounds and anchoring protein
WO1996025147A1 (fr) * 1995-02-14 1996-08-22 Sequus Pharmaceuticals, Inc. Composition de liposomes et procede d'administration de medicaments par liposomes
WO1996032930A1 (fr) * 1995-04-18 1996-10-24 Yissum Research Development Company Of The Hebrew University Of Jerusalem Procede de chargement de medicaments dans des liposomes et composition
US5939096A (en) * 1995-04-18 1999-08-17 Yissum Research Development Company Of The Hebrew University Of Jerusalem Liposome drug-loading method and composition
US5795735A (en) * 1995-07-17 1998-08-18 Icos Corporation Isolated polynucleotides encoding PKA-binding proteins and methods of producing the proteins recombinantly
US5994304A (en) * 1995-07-17 1999-11-30 Icos Corporation PKA-binding proteins and uses thereof
US5882910A (en) * 1996-11-25 1999-03-16 Icos Corporation Lipid kinase
US5858753A (en) * 1996-11-25 1999-01-12 Icos Corporation Lipid kinase
US5985589A (en) * 1996-11-25 1999-11-16 Icos Corporation Lipid kinase
US6090929A (en) * 1996-12-19 2000-07-18 Oregon Health Science University Protein binding fragments of gravin
US5741890A (en) * 1996-12-19 1998-04-21 Oregon Health Sciences University Protein binding fragments of gravin
US7244743B2 (en) * 2002-06-05 2007-07-17 Solvay Pharmaceuticals Gmbh Non-peptidic BRS-3 agonists
WO2004047802A2 (fr) * 2002-11-26 2004-06-10 Gilead Sciences, Inc. Formulations liposomiques
WO2004047802A3 (fr) * 2002-11-26 2004-09-23 Gilead Sciences Inc Formulations liposomiques
CN1938048B (zh) * 2004-03-26 2010-05-12 泰尔茂株式会社 脂质体制剂
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AU660288B2 (en) 1995-06-22
ES2089227T3 (es) 1996-10-01
ATE138803T1 (de) 1996-06-15
JP3533215B2 (ja) 2004-05-31
EP0555229B1 (fr) 1996-06-05
DK0555229T3 (da) 1996-08-19
DE69120089T2 (de) 1996-12-12
EP0555229A4 (fr) 1993-06-16
EP0555229A1 (fr) 1993-08-18
JPH06501246A (ja) 1994-02-10
CA2087965A1 (fr) 1992-02-01

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